Journal
CANCER IMMUNOLOGY IMMUNOTHERAPY
Volume 56, Issue 11, Pages 1831-1843Publisher
SPRINGER
DOI: 10.1007/s00262-007-0327-y
Keywords
dendritic cells; cytokines; chemokines; tumor immunology; gene therapy
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Dendritic cells play an important role in initiation and regulation of immune responses. Previous studies demonstrated that intratumoral administration of 6Ckine-modified DCs enhanced local and systemic antitumor effects. Herein we report the investigation of the specific CTL responses elicited by adenoviral 6Ckine/IFN gamma fusion gene-modified DCs in vitro. Human monocyte-derived DCs were modified with an adenoviral vector encoding 6Ckine/IFN gamma fusion protein (Ad-6Ckine/IFN gamma), and then investigated the effect of 6Ckine/IFN gamma fusion protein on the maturation, cytokine and chemokine secretion of DCs, and their activities of recruiting and activating T cells in vitro were investigated. 6Ckine/IFN gamma fusion protein induced DC maturation characterized with the upregulation of CD83 and CCR7. And it up-regulated the expression of RANTES and IL-12p70, down-regulated that of IL-10 in DCs. Additionally, 6Ckine/IFN gamma markedly increased DC's recruiting ability for naive T cells, benefiting from the enhanced expression of chemokines 6Ckine and RANTES in DCs. Fusion gene-modified DCs significantly promoted the proliferation of autologous T cells, induced Th1 differentiation by upregulating the expression of IL-2 and T-bet in T cells, and increased specific cytotoxicity of CTLs against specific tumor cells, HepG2 or LoVo cells, respectively. Combining the effects of 6Ckine and IFN gamma, Ad-6Ckine/IFN gamma modified DCs induced enhanced CTL responses in vitro, which indicated that Ad-6Ckine/IFN gamma modified DCs might be used as an adjuvant to trigger an effective antitumor immune response.
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